MYL3/CMLC1 抗体 (AA 1-195)
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- 抗原 See all MYL3/CMLC1 (MYL3) 抗体
- MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))
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抗原表位
- AA 1-195
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This MYL3/CMLC1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF)
- 序列
- MAPKKPEPKK DDAKAAPKAA PAPAPPPEPE RPKEVEFDAS KIKIEFTPEQ IEEFKEAFML FDRTPKCEMK ITYGQCGDVL RALGQNPTQA EVLRVLGKPR QEELNTKMMD FETFLPMLQH ISKNKDTGTY EDFVEGLRVF DKEGNGTVMG AELRHVLATL GERLTEDEVE KLMAGQEDSN GCINYEAFVK HIMSS
- 交叉反应
- 人, 小鼠, 大鼠
- 产品特性
- Polyclonal Antibodies
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-195 of human MYL3 (NP_000249.1).
- 亚型
- IgG
- Top Product
- Discover our top product MYL3 Primary Antibody
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- 应用备注
- WB,1:500 - 1:2000,IF,1:50 - 1:200
- 说明
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HIGH QUALITY
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))
- 别名
- MYL3 (MYL3 产品)
- 别名
- CMD1S antibody, CMH1 antibody, MPD1 antibody, MYHCB antibody, SPMD antibody, SPMM antibody, B-MHC antibody, MyHC-I antibody, Myhc-b antibody, Myhcb antibody, beta-MHC antibody, MLC1s antibody, MLC1v antibody, Mylc antibody, VLC1 antibody, Mylc1v antibody, CMH8 antibody, MLC1SB antibody, MLC1V antibody, mlc1v antibody, myl3-a antibody, myl3-b antibody, myl3.L antibody, zgc:103441 antibody, myosin heavy chain 7 antibody, myosin, heavy polypeptide 7, cardiac muscle, beta antibody, myosin, light polypeptide 3 antibody, myosin light chain 3 antibody, myosin light chain 3 S homeolog antibody, cardiac myosin light chain-1 antibody, MYH7 antibody, Myh7 antibody, Myl3 antibody, MYL3 antibody, myl3.S antibody, cmlc1 antibody
- 背景
- MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.,MYL3,CMH8,MLC-lV/sb,MLC1SB,MLC1V,VLC1,VLCl,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,Actins,Cardiovascular,Heart,Contractility,MYL3
- 分子量
- 21 kDa
- 基因ID
- 4634
- UniProt
- P08590
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